Ozdilek B, Uluc K, Gunal DI. Bilateral striopallidodentate calcinosis presenting with psychiatric symptoms and speech disorders. Background: Bilateral striopallidodentate calcinosis (BSPDC), also known as Fahr's disease, is a rare neurodegenerative disorder characterised by the deposition of calcium and other minerals in the basal ganglia, centrum semiovale and cerebellum. It is usually idiopathic. Its clinical manifestations vary from asymptomatic individuals to neuropsychiatric abnormalities, movement disorders, cerebellar symptoms and cognitive impairments. Methods: Five cases of BSPDC all of which include psychiatric symptoms and speech problems from two families are documented in this article. Conclusion: The most important diagnostic ...
Copyright © 2014 Rocco Salvatore Calabro ̀ et al.This is an open access article distributed under th...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...
Fahr’s disease is a rare inherited or sporadic neurological disorder with a prevalence of <1/1,000,0...
Bilateral striopallidodentate calcinosis (BSPDC) mentioned in the literature as Fahr's disease (a mi...
Bilateral striatopallidodentat kalsinozisle (BSPDK) nadir görülen, çeşitli semptomların bir arada g...
Fehr's disease, also known as Idiopathic Calcification of the Basal Ganglia (ICBG) or nonarterioscle...
OBJECTIVE: Bilateral basal ganglia calcification is a rare disease with symmetrical and bilateral de...
Familial idiopathic bilateral strio-pallido-dentate calcinosis is a rare autosomal dominant disorder...
WOS: 000363969000028Bilateral Striopallidodentat Calcinosis also called Fahr's disease (FH); basal g...
disease), is a rare syndrome characterized by symmetrical calcification over the basal ganglion and ...
DergiPark: 379009tmsjAims: Fahr’s disease is characterized by a bilateral striopallidodentate calcin...
Striato-pallido-dentate calcifications (SPDC) is a well defined entity, characterized by calcium dep...
AbstractParoxysmal kinesigenic dyskinesia (PKD) is presented as a short paroxysmal attack of focal o...
Fahr’s syndrome is a rare neurodegenerative disorder characterized by bilateral basal ganglia calcif...
Bilateral striopallidodentate calcification, usually termed Fahr's disease, can give rise to various...
Copyright © 2014 Rocco Salvatore Calabro ̀ et al.This is an open access article distributed under th...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...
Fahr’s disease is a rare inherited or sporadic neurological disorder with a prevalence of <1/1,000,0...
Bilateral striopallidodentate calcinosis (BSPDC) mentioned in the literature as Fahr's disease (a mi...
Bilateral striatopallidodentat kalsinozisle (BSPDK) nadir görülen, çeşitli semptomların bir arada g...
Fehr's disease, also known as Idiopathic Calcification of the Basal Ganglia (ICBG) or nonarterioscle...
OBJECTIVE: Bilateral basal ganglia calcification is a rare disease with symmetrical and bilateral de...
Familial idiopathic bilateral strio-pallido-dentate calcinosis is a rare autosomal dominant disorder...
WOS: 000363969000028Bilateral Striopallidodentat Calcinosis also called Fahr's disease (FH); basal g...
disease), is a rare syndrome characterized by symmetrical calcification over the basal ganglion and ...
DergiPark: 379009tmsjAims: Fahr’s disease is characterized by a bilateral striopallidodentate calcin...
Striato-pallido-dentate calcifications (SPDC) is a well defined entity, characterized by calcium dep...
AbstractParoxysmal kinesigenic dyskinesia (PKD) is presented as a short paroxysmal attack of focal o...
Fahr’s syndrome is a rare neurodegenerative disorder characterized by bilateral basal ganglia calcif...
Bilateral striopallidodentate calcification, usually termed Fahr's disease, can give rise to various...
Copyright © 2014 Rocco Salvatore Calabro ̀ et al.This is an open access article distributed under th...
Fahr’s disease (FD) is characterized by sporadic or familiar idiopathic calcification of the basal g...
Fahr’s disease is a rare inherited or sporadic neurological disorder with a prevalence of <1/1,000,0...